Abstract (R)-(1-Naphthyl)glycyl-(R)-phenylglycine forms inclusion compounds with ethers (tetrahydrofuran and diethyl ether) or allylic alcohols (2-propen-1-ol and 2-methyl-2-propen-1-ol). X-ray crystallographic study showed that the dipeptide has the ability to optionally form “parallel or antiparallel” β-sheet-like structures by the choice of ethers or allylic alcohols, respectively, as the guest molecules.
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Akazome et al. (1996) studied this question.
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